An information theoretic approach for selecting arms in clinical trials

被引:11
|
作者
Mozgunov, Pavel [1 ]
Jaki, Thomas [1 ,2 ]
机构
[1] Univ Lancaster, Lancaster, England
[2] Univ Cambridge, Cambridge, England
基金
英国医学研究理事会; 美国国家卫生研究院; 欧盟地平线“2020”;
关键词
Dose finding; Experimental design; Information gain; Multinomial outcomes; Response-adaptive design; Shannon's differential entropy; ADAPTIVE RANDOMIZATION; OPTIMAL-DESIGN; GITTINS INDEX; ALLOCATION;
D O I
10.1111/rssb.12391
中图分类号
O21 [概率论与数理统计]; C8 [统计学];
学科分类号
020208 ; 070103 ; 0714 ;
摘要
The question of selecting the 'best' among different choices is a common problem in statistics. In drug development, our motivating setting, the question becomes, for example, which treatment gives the best response rate. Motivated by recent developments in the theory of context-dependent information measures, we propose a flexible response-adaptive experimental design based on a novel criterion governing treatment arm selections which can be used in adaptive experiments with simple (e.g. binary) and complex (e.g. co-primary, ordinal or nested) end points. It was found that, for specific choices of the context-dependent measure, the criterion leads to a reliable selection of the correct arm without any parametric or monotonicity assumptions and provides noticeable gains in settings with costly observations. The asymptotic properties of the design are studied for different allocation rules, and the small sample size behaviour is evaluated in simulations in the context of phase II clinical trials with different end points. We compare the proposed design with currently used alternatives and discuss its practical implementation.
引用
收藏
页码:1223 / 1247
页数:25
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